<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kumar M</submitter><funding>European Research Council</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>16753-16756</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6348375</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(63)</volume><pubmed_abstract>The inthomycins are a family of structurally and biologically rich natural products isolated from Streptomyces species. Herein the implementation of a modular synthetic route is reported that has enabled the enantioselective synthesis of all three inthomycins. Key steps include Suzuki and Sonogashira cross-couplings and an enantioselective Kiyooka aldol reaction.</pubmed_abstract><journal>Chemistry (Weinheim an der Bergstrasse, Germany)</journal><pubmed_title>Short, Tin-Free Synthesis of All Three Inthomycins.</pubmed_title><pmcid>PMC6348375</pmcid><funding_grant_id>708354</funding_grant_id><funding_grant_id>EP/J004499/1</funding_grant_id><pubmed_authors>Anderson Z</pubmed_authors><pubmed_authors>Kumar M</pubmed_authors><pubmed_authors>Overy A</pubmed_authors><pubmed_authors>Burton JW</pubmed_authors><pubmed_authors>Bromhead L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Short, Tin-Free Synthesis of All Three Inthomycins.</name><description>The inthomycins are a family of structurally and biologically rich natural products isolated from Streptomyces species. Herein the implementation of a modular synthetic route is reported that has enabled the enantioselective synthesis of all three inthomycins. Key steps include Suzuki and Sonogashira cross-couplings and an enantioselective Kiyooka aldol reaction.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2026-05-07T06:29:22.162Z</modification><creation>2025-05-29T22:28:48.278Z</creation></dates><accession>S-EPMC6348375</accession><cross_references><pubmed>30338587</pubmed><doi>10.1002/chem.201803794</doi></cross_references></HashMap>